56870-03-2 Usage
Uses
Used in Pharmaceutical Industry:
2-Propanone, 1-chloro-1-(methylthio)is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its reactivity in nucleophilic substitution reactions allows for the creation of a wide range of drug molecules, contributing to the development of new treatments and medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Propanone, 1-chloro-1-(methylthio)is employed as a building block for the production of various agrochemicals. Its ability to participate in organic synthesis reactions enables the creation of effective pesticides and other agricultural chemicals that protect crops and enhance agricultural productivity.
Used as a Solvent:
2-Propanone, 1-chloro-1-(methylthio)is utilized as a solvent in various chemical processes due to its ability to dissolve a wide range of substances. Its solvent properties make it a valuable component in the chemical industry for processes that require the dissolution of solids or the facilitation of chemical reactions.
Used in Rubber and Plastics Manufacturing:
This chemical compound is also used in the manufacturing of rubber and plastics, where its reactivity and properties contribute to the formation of desired material characteristics. Its involvement in the production process helps to create rubber and plastic products with specific properties tailored to various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 56870-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,7 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56870-03:
(7*5)+(6*6)+(5*8)+(4*7)+(3*0)+(2*0)+(1*3)=142
142 % 10 = 2
So 56870-03-2 is a valid CAS Registry Number.
56870-03-2Relevant academic research and scientific papers
Syntheses of Arylacetone and Arylacetonitrile by Friedel-Crafts Reaction with α-Chloro-α-(methylthio)-substituted Acetone and Acetonitrile
Tamura, Yasumitsu,Choi, Hong Dae,Mizutani, Masako,Ueda, Yuko,Ishibashi, Hiroyuki
, p. 3574 - 3579 (2007/10/02)
Novel preparative methods for arylacetone and arylacetonitrile are described.Friedel-Crafts reactions of aromatic compounds with α-chloro-α-(methylthio)acetone (4) and α-chloro-α-(methylthio)acetonitrile (7) in the presence of Lewis acid afforded α-(methylthio)arylacetone (5) and α-(methylthio)arylacetonitrile (8), respectively.Compounds (5) and (8) were converted into the corresponding arylacetone (6) and arylacetonitrile (9) by reduction with zinc dust in acetic acid.Keywords: Friedel-Crafts reaction with α-chloro-α-(methylthio)acetone; Friedel-Crafts reaction with α-chloro-α-(methylthio)acetonitrile; α-(methylthio)arylacetone; α-(methylthio)arylacetonitrile; arylacetone; arylacetonitrile; reductive desulfurization; zinc dust-acetic acid
